Phelan Mfg Corp

Form 483FOIA Uncovered

Minneapolis, Minnesota, United StatesFEI 2126376Issued April 18, 2019

View FDA's Record for This Firm

Source: FDA inspection record. Confirmed against FDA's published inspection data for this establishment and inspection date. FDA has published the inspection and what it cited, but not the form itself, which usually takes six to twelve months. To check it, open FDA's record for this establishment on FDA's Data Dashboard, listed under FEI 2126376.

Observations1

Issue DateApril 18, 2019

StatusNo Warning Letter

Related Inspections2

Establishment Details

Firm: Phelan Mfg Corp
Location: Minneapolis, Minnesota, United States
FEI Number: 2126376
Product Type: Devices
Issue Date: April 18, 2019
Country: United States

Inspection History, 2015 to 2019

NAI1

VAI1

NAI means No Action Indicated. VAI means Voluntary Action Indicated.

Act on This Form 483

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Phelan Mfg Corp FDA Form 483, Minneapolis, Minnesota, April 18, 2019